Canonical Allele Identifier: CA796273306

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.53794991A>T , CM000666.2:g.53794991A>T	GRCh38
NC_000004.11:g.54661158A>T , CM000666.1:g.54661158A>T	GRCh37
NC_000004.10:g.54355915A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507166.5:c.1017+369026A>T	ENSP00000423325.1:n.1017+369026A>T